meddevicedb.com FDA Device Reference

IRON LIQUID STABLE REAGENT

K900902 Class I Traditional
Decision Date
1990-03-19
Sponsor / Applicant
Medical Analysis Systems, Inc.

Technical Specification

510(k) Submission ID K900902
Product Code JIY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1410
Decision Date 1990-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRON LIQUID STABLE REAGENT received FDA 510(k) clearance under submission number K900902, sponsored by Medical Analysis Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1990-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code JIY and 21 CFR 862.1410, within the Clinical Chemistry review panel as a Class I device.